Please use this identifier to cite or link to this item: http://ktisis.cut.ac.cy/handle/10488/4358
Title: First-trimester ductus venosus screening for cardiac defects: a meta-analysis
Authors: Papatheodorou, Stefania ItemCrisRefDisplayStrategy.rp.deleted.icon
Makrydimas, George V.
Ioannidis, John P. A. 
Evangelou, Evangelos ItemCrisRefDisplayStrategy.rp.deleted.icon
Keywords: Chromosomal abnormalities;Congenital heart disease;Ductus venosus;Nuchal translucency
Category: Clinical Medicine
Field: Medical and Health Sciences
Issue Date: Nov-2011
Publisher: John Wiley & Sons, Inc.
Source: BJOG: An International Journal of Obstetrics and Gynaecology, 2011, Volume 118, Issue 12, Pages 1438-1445
Abstract: Background Heart defects are the most common congenital abnormalities. Objective We aimed to evaluate in a meta-analysis the screening performance of abnormal ductus venosus (DV) Doppler waveform for detection of congenital heart disease (CHD) in chromosomally normal fetuses. Search strategy Studies were retrieved from a search of MEDLINE, ISI, SCOPUS and EMBASE (from 1999 to March 2011) using the keywords 'ductus venosus', 'DV', 'chromosomal abnormalities', 'congenital heart disease' and 'nuchal translucency'. Selection criteria We considered all studies that examined the diagnostic performance of DV in the first trimester for CHD in chromosomally normal fetuses. We included studies that were limited to fetuses with increased nuchal translucency (NT), normal NT, and studies that examined fetuses regardless of NT status. Data collection and analysis Seven studies (n = 50 354) regardless of the NT status, nine studies (n = 2908) with increased NT and seven studies (n = 47 610) with normal NT were included in the meta-analysis. We drew hierarchical summary receiver operating characteristic (HSROC) curves using the parameters of the fitted models. Main results In populations including participants regardless of NT status, the summary sensitivity and specificity of DV for detecting CHD were 50 and 93%, respectively. In participants with increased NT, the summary sensitivity and specificity were 83 and 80%, and in those with normal NT, they were 19 and 96%, respectively. Authors' conclusions The estimated performance of DV assessment for detection of CHD in chromosomally normal fetuses can be considered in evaluating the potential use and limitations of this screening test.
URI: http://ktisis.cut.ac.cy/handle/10488/4358
http://hdl.handle.net/10488/4358
ISSN: 1471-0528
DOI: 10.1111/j.1471-0528.2011.03029.x
Rights: © The Authors BJOG An International Journal of Obstetrics and Gynaecology
Type: Article
Appears in Collections:Άρθρα/Articles

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